Papers associated with posterior hypothalamus (and ctnnb1)

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	Adenomatous polyposis coli tumor suppressor protein has signaling activity in Xenopus laevis embryos resulting in the induction of an ectopic dorsoanterior axis., Vleminckx K, Vleminckx K., J Cell Biol. January 27, 1997; 136 (2): 411-20.
	Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos., Salic AN., Development. December 1, 1997; 124 (23): 4739-48.
	LEF-1/TCF proteins mediate wnt-inducible transcription from the Xenopus nodal-related 3 promoter., McKendry R., Dev Biol. December 15, 1997; 192 (2): 420-31.
	Pre-MBT patterning of early gene regulation in Xenopus: the role of the cortical rotation and mesoderm induction., Ding X., Mech Dev. January 1, 1998; 70 (1-2): 15-24.
	Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand., Jones TL., Proc Natl Acad Sci U S A. January 20, 1998; 95 (2): 576-81.
	The juxtamembrane region of the cadherin cytoplasmic tail supports lateral clustering, adhesive strengthening, and interaction with p120ctn., Yap AS., J Cell Biol. May 4, 1998; 141 (3): 779-89.
	Effects of forced expression of an NH2-terminal truncated beta-Catenin on mouse intestinal epithelial homeostasis., Wong MH., J Cell Biol. May 4, 1998; 141 (3): 765-77.
	Negative regulation of axis formation and Wnt signaling in Xenopus embryos by the F-box/WD40 protein beta TrCP., Lagna G., Mech Dev. January 1, 1999; 80 (1): 101-6.
	Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF., Dev Biol. March 15, 1999; 207 (2): 350-63.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	A cell-free assay system for beta-catenin signaling that recapitulates direct inductive events in the early xenopus laevis embryo., Nelson RW., J Cell Biol. October 18, 1999; 147 (2): 367-74.
	Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development., Baker JC., Genes Dev. December 1, 1999; 13 (23): 3149-59.
	The transcriptional coactivator CBP interacts with beta-catenin to activate gene expression., Takemaru KI., J Cell Biol. April 17, 2000; 149 (2): 249-54.
	Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach., Heasman J., Dev Biol. June 1, 2000; 222 (1): 124-34.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	A novel beta-catenin-binding protein inhibits beta-catenin-dependent Tcf activation and axis formation., Sakamoto I., J Biol Chem. October 20, 2000; 275 (42): 32871-8.
	Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus., Wessely O., Dev Biol. June 1, 2001; 234 (1): 161-73.
	Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.
	Timing of endogenous activin-like signals and regional specification of the Xenopus embryo., Lee MA., Development. August 1, 2001; 128 (15): 2939-52.
	The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	Sox17 and beta-catenin cooperate to regulate the transcription of endodermal genes., Sinner D., Development. July 1, 2004; 131 (13): 3069-80.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation., Daniels M., Development. November 1, 2004; 131 (22): 5613-26.
	PR72, a novel regulator of Wnt signaling required for Naked cuticle function., Creyghton MP., Genes Dev. February 1, 2005; 19 (3): 376-86.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	Kaiso/p120-catenin and TCF/beta-catenin complexes coordinately regulate canonical Wnt gene targets., Park JI., Dev Cell. June 1, 2005; 8 (6): 843-54.
	xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O., Dev Biol. July 1, 2005; 283 (1): 17-28.
	Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK., Cell Commun Signal. October 19, 2005; 3 12.
	RanBP3 enhances nuclear export of active (beta)-catenin independently of CRM1., Hendriksen J., J Cell Biol. December 5, 2005; 171 (5): 785-97.
	HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	NARF, an nemo-like kinase (NLK)-associated ring finger protein regulates the ubiquitylation and degradation of T cell factor/lymphoid enhancer factor (TCF/LEF)., Yamada M., J Biol Chem. July 28, 2006; 281 (30): 20749-20760.
	Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.
	Intracellular expression profiles measured by real-time PCR tomography in the Xenopus laevis oocyte., Sindelka R., Nucleic Acids Res. February 1, 2008; 36 (2): 387-92.
	Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.
	Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo., Li S., Differentiation. October 1, 2008; 76 (8): 897-907.
	Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL., Chitalia VC., Nat Cell Biol. October 1, 2008; 10 (10): 1208-16.
	Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation., Cha SW., Development. November 1, 2008; 135 (22): 3719-29.
	Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
	Inhibition of GSK3 phosphorylation of beta-catenin via phosphorylated PPPSPXS motifs of Wnt coreceptor LRP6., Wu G., PLoS One. January 1, 2009; 4 (3): e4926.
	N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.
	Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis., Morita H., Development. April 1, 2010; 137 (8): 1315-25.
	Homeodomain-interacting protein kinase 2 (HIPK2) targets beta-catenin for phosphorylation and proteasomal degradation., Kim EA., Biochem Biophys Res Commun. April 16, 2010; 394 (4): 966-71.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.

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